DRB3 alleles with variations in the annealing sites of commonly used amplification primers

Tissue Antigens. 2000 Jun;55(6):558-63. doi: 10.1034/j.1399-0039.2000.550606.x.

Abstract

New HLA alleles are often identified initially from observing uncommon patterns found in low-resolution typing performed via polymerase chain reaction using sequence-specific oligonucleotide probes (PCR-SSOP). Recently, the HLA-DR oligotyping analysis of two Caucasian, one Caucasian/American Indian and two African American individuals resulted in the identification of three novel DRB3 alleles. Using DRB-specific primer sets commonly employed in amplification-based typing, all four individuals were originally characterized as DRB3 negative. Direct sequencing identified DRB3*0104 (variation at codon 8, TCG instead of TTG), and DRB3*0101202 (variation at intron (-13), G instead of C). One individual appeared to carry a DR52-associated DRB1 allele without an associated DRB3 allele. Lack of conservation at the junction of intron 1 and exon 2 of the DRB3 gene suggests that commonly used DRB-specific primer sets may need to be modified.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Alleles*
  • Base Pairing / genetics*
  • Base Sequence
  • DNA Primers* / chemical synthesis
  • DNA Primers* / metabolism
  • Gene Amplification*
  • Genetic Variation / immunology*
  • HLA-DR Antigens / genetics*
  • HLA-DRB3 Chains
  • Histocompatibility Testing
  • Humans
  • Molecular Sequence Data
  • Nucleic Acid Amplification Techniques

Substances

  • DNA Primers
  • HLA-DR Antigens
  • HLA-DRB3 Chains